Memorial Sloan Kettering Cancer Center, New York, New York.
Weill Cornell Medical College, New York, New York.
J Clin Oncol. 2020 May 20;38(15):1655-1663. doi: 10.1200/JCO.19.01464. Epub 2020 Feb 13.
To analyze long-term outcomes after treatment discontinuation of anti-programmed death-1 (anti-PD-1) therapy in a cohort of patients with melanoma with the longest follow-up yet available to our knowledge, including a majority of patients treated outside of a clinical trial. We also assessed efficacy of retreatment with anti-PD-1 therapy with or without ipilimumab in relapsing patients.
We retrospectively analyzed all patients with nonuveal, unresectable stage III/IV melanoma treated with single-agent anti-PD-1 therapy at Memorial Sloan Kettering from 2009-2018 who had discontinued treatment and had at least 3 months of follow-up after discontinuation (n = 396). Overall survival for patients with complete response (CR) was calculated from time of CR. Time to treatment failure for patients with CR was time from CR to the next melanoma treatment or death.
CRs were seen in 102 of 396 patients (25.8%). The median number of months of treatment after CR was zero (range, stopped before CR to 26 months after CR). With a median follow-up of 21.1 months from time of CR in patients who did not relapse, the probability of being alive and not needing additional melanoma therapy at 3 years was 72.1%. There was no significant association between treatment duration and relapse risk. In multivariable analysis, CR was associated with M1b disease and cutaneous versus mucosal or acral primaries. Among the 78 patients (of 396) retreated after disease progression, response was seen in 5 of 34 retreated patients with single-agent anti-PD-1 therapy and 11 of 44 patients escalated to anti-PD-1 plus ipilimumab.
In our cohort, most patients discontinued treatment at the time of CR. Most CRs were durable but the probability of treatment failure was 27% at 3 years. Responses to retreatment were infrequent. The optimal duration of treatment after CR is not yet established.
分析迄今为止我们所了解的黑色素瘤患者队列中抗程序性死亡-1(抗 PD-1)治疗停药后的长期结果,包括大多数在临床试验之外接受治疗的患者。我们还评估了复发患者再次接受抗 PD-1 治疗联合或不联合伊匹单抗的疗效。
我们回顾性分析了 2009 年至 2018 年期间在 Memorial Sloan Kettering 接受单药抗 PD-1 治疗的非眼、不可切除的 III/IV 期黑色素瘤患者的所有数据,这些患者停药且停药后至少有 3 个月的随访(n = 396)。完全缓解(CR)患者的总生存时间从 CR 时间开始计算。CR 患者的治疗失败时间从 CR 到下一次黑色素瘤治疗或死亡的时间。
396 例患者中 102 例(25.8%)出现 CR。CR 后治疗的中位月数为零(范围为 CR 前停止治疗至 CR 后 26 个月)。在未复发的 CR 患者中,中位随访 21.1 个月后,3 年时无病生存且无需额外黑色素瘤治疗的概率为 72.1%。治疗持续时间与复发风险之间无显著相关性。多变量分析显示,CR 与 M1b 疾病以及皮肤 vs 黏膜或肢端原发性疾病相关。在 78 例(396 例)疾病进展后接受治疗的患者中,5 例接受单药抗 PD-1 治疗的患者和 44 例升级为抗 PD-1 联合伊匹单抗治疗的患者中有 11 例出现缓解。
在我们的队列中,大多数患者在 CR 时停止治疗。大多数 CR 是持久的,但 3 年时治疗失败的概率为 27%。对再次治疗的反应不频繁。CR 后最佳治疗持续时间尚未确定。